4.6 Article

Efficacy of theobromine in preventing intestinal CaCo-2 cell damage induced by oxysterols

Journal

ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS
Volume 694, Issue -, Pages -

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.abb.2020.108591

Keywords

Apoptosis; Dietary oxysterols; Intestinal inflammation; Tight junctions; Matrix metalloproteinases; Theobromine

Funding

  1. Universita degli Studi di Torino (IT) [BIAF_RILO_17_01, BIAF_RILO_18_01]
  2. Ministero dell'Istruzione, dell'Universita e della Ricerca (IT) [BIAF_FFABR_17_01]

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The alteration of the intestinal barrier function is currently believed to be involved in the pathogenesis of gut diseases mainly associated with the activation of inflammation processes. Diet plays an important role in the control of human gut integrity. Theobromine is a natural methylxanthine present in dark chocolate particularly abundant in cocoa bean shell. This is a polyphenol rich by-product generated in cocoa industrial processing, which is gaining value as a functional ingredient. This study aims to highlight for the first time the capability of theobromine in protecting the intestinal cell monolayer from a mixture of dietary oxysterols showing an inflammatory action in terms of IL-8 and MCP-1 overproduction. Differentiated CaCo-2 cells were treated with 60 mu M oxysterol mixture and pre-incubated with 10 mu M theobromine. Intestinal barrier damage was investigated in terms of tight junction claudin 1, occludin and JAM-A protein levels, matrix metalloproteinase (MMP) 2 and 9 activation and anti/pro-apoptotic protein changes. The observed cell monolayer permeability protection by theobromine may be due to its ability to inhibit the production of cytokines and MMPs that can be responsible for tight junction loss and apoptosis in intestinal cells. Our findings provide additional mechanistic hints on the healthy effect of theobromine cocoa component as an attractive natural molecule in the prevention of inflammatory gut diseases.

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